Pilz, D T <br/><br/>
Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics   
 - 29-33 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-3600 
<br/><br/><label>Standard No.: </label>10.1097/00125817-199811000-00007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>1-Alkyl-2-acetylglycerophosphocholine Esterase<br/>Brain--abnormalities<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Gene Deletion<br/>Genetic Markers<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Microtubule-Associated Proteins--genetics<br/>Mutation